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The Contribution of cocoa additive to cigarette smoking addiction

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RIVM report 650270002 Page 95 <strong>of</strong> 207<br />

Tryp<strong>to</strong>phan<br />

<strong>smoking</strong> will significantly affect the tryp<strong>to</strong>phan plasma level.<br />

PHARMACODYNAMICS<br />

Mechanism <strong>of</strong> action<br />

Tryp<strong>to</strong>phan is an essential constituent <strong>of</strong> the diet. It plays an important role in protein<br />

synthesis and is also precursor <strong>of</strong> a variety <strong>of</strong> biologically active compounds<br />

including sero<strong>to</strong>nin, mela<strong>to</strong>nin, tryptamine, quinolinic acid and kynurenic acid. In<br />

addition, tryp<strong>to</strong>phan is precursor <strong>to</strong> the coenzymes NAD and NADP and can replace<br />

niacin as an essential nutrient (10).<br />

A compound in <strong>cigarette</strong> tar, possibly an oxidised tryp<strong>to</strong>phan, exhibits an affinity for<br />

the aryl-hydrocarbon recep<strong>to</strong>r, which induces the biotransformation enzymes (16).<br />

Pulmonary system<br />

breathing frequency: no data available<br />

tidal volume: no data available<br />

lung compliance: no data available<br />

airway resistance: no data available<br />

Cardiovascular system<br />

blood pressure: In humans, single oral doses <strong>of</strong> L-tryp<strong>to</strong>phan (50 mg/kg body<br />

weight) lowered blood pressure significantly 90-120 min after administration in<br />

patients with essential hypertension, but not in normotensive controls. <strong>The</strong><br />

tryp<strong>to</strong>phan-induced lowering <strong>of</strong> blood pressure could be attributable <strong>to</strong> the<br />

enhancement <strong>of</strong> central sero<strong>to</strong>nin synthesis (17).<br />

Chronic oral administration <strong>of</strong> L-tryp<strong>to</strong>phan (1.26 g/kg/day) attenuated the elevation<br />

<strong>of</strong> sys<strong>to</strong>lic blood pressure in deoxycorticosterone salt-treated rats (18).<br />

heart rate: No data available.<br />

Renal system<br />

diuresis: Intra peri<strong>to</strong>neal injected tryp<strong>to</strong>phan in rats showed the same antidiuretic<br />

effect as sero<strong>to</strong>nin in rats; it has an initial antidiuretic effect and evokes<br />

subsequently diuresis (19).<br />

saluresis: Tryp<strong>to</strong>phan injected in the median raphe nucleus <strong>of</strong> rats (200 mg/kg)<br />

increased the Na + and K + excretion (20).<br />

Nervous system<br />

Tryp<strong>to</strong>phan affects the CNS due <strong>to</strong> alternations <strong>of</strong> brain tryp<strong>to</strong>phan levels, which<br />

influence sero<strong>to</strong>nin synthesis (10). Both excessive intake and deficiency <strong>of</strong><br />

tryp<strong>to</strong>phan affects the CNS.<br />

central nervous system: Tryp<strong>to</strong>phan deficiency (due <strong>to</strong> chronic dietary<br />

insufficiency) may lead <strong>to</strong> pellagra. Pellagra is associated with diarrhoea,<br />

dermatitis and mental symp<strong>to</strong>ms. Mild cases <strong>of</strong> pellagra can be associated with<br />

headache, sleep disturbances and depression and severe cases are associated with<br />

hallucinations, cata<strong>to</strong>nia, dementia and seizures. Tryp<strong>to</strong>phan is used in mild <strong>to</strong><br />

moderate depression, mild insomnia, pain and aggression. High oral doses (> 1 g)<br />

are needed <strong>to</strong> obtain these pharmacological effects (10).<br />

au<strong>to</strong>nomic system: No data available.

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